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Solvent effect on the absorption and emission spectra of carbon dots: evaluation of ground and excited state dipole moment

Authors :
Parisa Mohammad-Jafarieh
Abolfazl Akbarzadeh
Rahman Salamat-Ahangari
Mohammad Pourhassan-Moghaddam
Kazem Jamshidi-Ghaleh
Source :
BMC Chemistry, Vol 15, Iss 1, Pp 1-10 (2021)
Publication Year :
2021
Publisher :
BMC, 2021.

Abstract

Abstract Background Carbon dots (C-dots) are photoluminescent nanoparticles with less than 10 nm in size. Today, many studies are performed to exploit the photoluminescence (PL) property of carbon dots, and our focus in this study is to estimate the dipole moment of carbon dots. For reaching our aims, C-dots were synthesized and dissolved in the different solvents. Results Carbon dots with intense photoluminescence properties have been synthesized by a one-step hydrothermal method from a carbon bio-source. In this research, we report on the effect of aprotic solvents on absorption and fluorescence spectra and dipole moments of C-dots dispersed in a range of many aprotic solvents with various polarity and dielectric constant at room temperature. The change in the value of dipole moment was estimated by using the Stokes shifts. The difference between the dipole moment of the excited state and the ground state was shown using an extended form of Lippert equations by Kawski and co-workers. Conclusions The values found for μg = 1.077 D, and μe = 3.157 D, as well as the change in the dipole moments. The results showed that the dipole moment of the excited state is more than the ground state, indicating a high density and redistribution of electrons in the excited state. Finally, the quantum yield of C-dots in the eclectic aprotic solvents was communicated and discussed.

Details

Language :
English
ISSN :
2661801X
Volume :
15
Issue :
1
Database :
Directory of Open Access Journals
Journal :
BMC Chemistry
Publication Type :
Academic Journal
Accession number :
edsdoj.36f051e497b4de38bc5f9b55a497104
Document Type :
article
Full Text :
https://doi.org/10.1186/s13065-021-00779-6